Porosity as a Design Element for Developing Catalytic Molecular Materials for Electrochemical and Photochemical Carbon Dioxide Reduction

被引:21
作者
de la Torre, Patricia [1 ,2 ]
An, Lun [1 ,2 ]
Chang, Christopher J. [1 ,2 ,3 ]
机构
[1] Univ Calif Berkeley, Dept Chem, Berkeley, CA 94720 USA
[2] Lawrence Berkeley Natl Lab, Chem Sci Div, Berkeley, CA 94720 USA
[3] Univ Calif Berkeley, Dept Mol & Cell Biol, Berkeley, CA 94720 USA
关键词
carbon dioxide reduction; catalysis; molecular materials; porosity; METAL-ORGANIC FRAMEWORKS; CO2; REDUCTION; SELECTIVE CO2; RETICULAR CHEMISTRY; ELECTROCATALYTIC REDUCTION; ELECTRON TRANSMISSION; COBALT PORPHYRINS; IRON; ELECTROREDUCTION; CONVERSION;
D O I
10.1002/adma.202302122
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The catalytic reduction of carbon dioxide (CO2) using sustainable energy inputs is a promising strategy for upcycling of atmospheric carbon into value-added chemical products. This goal has inspired the development of catalysts for selective and efficient CO2 conversion using electrochemical and photochemical methods. Among the diverse array of catalyst systems designed for this purpose, 2D and 3D platforms that feature porosity offer the potential to combine carbon capture and conversion. Included are covalent organic frameworks (COFs), metal-organic frameworks (MOFs), porous molecular cages, and other hybrid molecular materials developed to increase active site exposure, stability, and water compatibility while maintaining precise molecular tunability. This mini-review showcases catalysts for the CO2 reduction reaction (CO2RR) that incorporate well-defined molecular elements integrated into porous materials structures. Selected examples provide insights into how different approaches to this overall design strategy can augment their electrocatalytic and/or photocatalytic CO2 reduction activity.
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页数:14
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